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rs13306487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs13306487(A;A)
Make rs13306487(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position47292422
GeneITGB3
is asnp
is mentioned by
dbSNPrs13306487
ebirs13306487
HLIrs13306487
Exacrs13306487
Varsomers13306487
Maprs13306487
PheGenIrs13306487
hapmaprs13306487
1000 genomesrs13306487
hgdprs13306487
ensemblrs13306487
gopubmedrs13306487
geneviewrs13306487
scholarrs13306487
googlers13306487
pharmgkbrs13306487
gwascentralrs13306487
openSNPrs13306487
23andMers13306487
23andMe allrs13306487
SNP Nexus

SNPshotrs13306487
SNPdbers13306487
MSV3drs13306487
GWAS Ctlgrs13306487
GMAF0.006887
Max Magnitude0
OMIM173470
DescCa/Tu ALLOANTIGEN POLYMORPHISM
Variant0009
Relatedalso
ClinVar
Risk rs13306487(A,C;A,C)
Alt rs13306487(A,C;A,C)
Reference rs13306487(G;G)
Significance Pathogenic
Disease Ca/Tu ALLOANTIGEN POLYMORPHISM Thrombocytopenia
Variation info
Gene ITGB3
CLNDBN Ca/Tu ALLOANTIGEN POLYMORPHISM Thrombocytopenia, neonatal alloimmune
Reversed 0
HGVS NC_000017.10:g.45369788G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014528.2, RCV000014529.19,